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DO Term : multiple congenital anomalies-hypotonia-seizures syndrome [DOID:0080503] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  A lipid metabolism disorder that is characterized by severe global developmental delay, hypotonia, and early-onset seizures, associated with multiple cardiac, genitourinary, and gastrointestinal congenital anomalies.
  • synonyms:
  • ORDO:280633,
  • OMIM:PS614080,
  • GARD:12781,
  • PS614080
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Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents